Canonical Allele Identifier: CA1142265291
Gene: ACTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.229431441_229431447delinsCCCCCCC , CM000663.2:g.229431441_229431447delinsCCCCCCC GRCh38
NC_000001.10:g.229567188_229567194delinsCCCCCCC , CM000663.1:g.229567188_229567194delinsCCCCCCC GRCh37
NC_000001.9:g.227633811_227633817delinsCCCCCCC NCBI36
NG_006672.1:g.7650_7656delinsGGGGGGG , LRG_429:g.7650_7656delinsGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000366683.4:c.*52_*58delinsGGGGGGG ENSP00000355644.4:n.*52_*58delinsGGGGGGG
ENST00000684723.1:c.*52_*58delinsGGGGGGG ENSP00000508084.1:n.*52_*58delinsGGGGGGG
ENST00000366683.3:c.*52_*58delinsGGGGGGG ENSP00000355644.3:n.*52_*58delinsGGGGGGG
ENST00000366684.7:c.*52_*58delinsGGGGGGG MANE Select ENSP00000355645.3:n.*52_*58delinsGGGGGGG
NM_001100.3:c.*52_*58delinsGGGGGGG , LRG_429t1:c.*52_*58delinsGGGGGGG NP_001091.1:n.*52_*58delinsGGGGGGG
NM_001100.4:c.*52_*58delinsGGGGGGG MANE Select NP_001091.1:n.*52_*58delinsGGGGGGG